Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutations

Hypomorphic mutations of the RAG genes in humans are associated with a spectrum of clinical and immunologic presentations that range from T(−) B(−) severe combined immune deficiency (SCID) to Omenn syndrome. In most cases, residual V(D)J recombination activity allows for development of few T-cell cl...

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Detalhes bibliográficos
Main Authors: Matangkasombut, Ponpan, Pichavant, Muriel, Saez, Doris E., Giliani, Silvia, Mazzolari, Evelina, Finocchi, Andrea, Villa, Anna, Sobacchi, Cristina, Cortes, Patricia, Umetsu, Dale T., Notarangelo, Luigi D.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2008
Assuntos:
Immunobiology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2200812/
https://ncbi.nlm.nih.gov/pubmed/17890453
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2007-06-096487
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